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Silane, [(5,5-dimethyl-3-methylene-1-cyclohexen-1-yl)oxy]trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80239-27-6

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80239-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80239-27-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,3 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80239-27:
(7*8)+(6*0)+(5*2)+(4*3)+(3*9)+(2*2)+(1*7)=116
116 % 10 = 6
So 80239-27-6 is a valid CAS Registry Number.

80239-27-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (5,5-dimethyl-3-methylidenecyclohexen-1-yl)oxy-trimethylsilane

1.2 Other means of identification

Product number -
Other names Silane,[(5,5-dimethyl-3-methylene-1-cyclohexen-1-yl)oxy]trimethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80239-27-6 SDS

80239-27-6Relevant academic research and scientific papers

N-heterocyclic carbene-catalyzed silyl enol ether formation

Song, Jinhua J.,Tan, Zhulin,Reeves, Jonathan T.,Fandrick, Daniel R.,Yee, Nathan K.,Senanayake, Chris H.

supporting information; experimental part, p. 877 - 880 (2009/04/07)

N-Heterocyclic carbenes (NHCs) were found to catalyze the silyl transfer from trialkylsilyl ketene acetals to ketones. In the presence of a catalytic amount of NHC 3 (IAd, 0.1 to 5 mol%), a series of enolizable ketones as well as cyclohexanecarboxaldehyde

INTRAMOLECULAR PHOTOCYCLOADDITION OF ENONE-ACETALS

Pirrung, Michael C.,Thomson, Stephen A.

, p. 2703 - 2706 (2007/10/02)

Lewis acid catalyzed condensation of unsaturated orthoformates with dienol ethers gives enone-acetals suitable for intramolecular photocycloadditions, yielding heterocyclic precursors to sesquiterpene lactones.

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